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rs12485738

From SNPedia

Orientationplus
Stabilizedplus
Make rs12485738(A;A)
Make rs12485738(A;G)
Make rs12485738(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position56831748
GeneARHGEF3
is asnp
is mentioned by
dbSNPrs12485738
ebirs12485738
HLIrs12485738
Exacrs12485738
Varsomers12485738
Maprs12485738
PheGenIrs12485738
hapmaprs12485738
1000 genomesrs12485738
hgdprs12485738
ensemblrs12485738
gopubmedrs12485738
geneviewrs12485738
scholarrs12485738
googlers12485738
pharmgkbrs12485738
gwascentralrs12485738
openSNPrs12485738
23andMers12485738
23andMe allrs12485738
SNP Nexus

SNPshotrs12485738
SNPdbers12485738
MSV3drs12485738
GWAS Ctlgrs12485738
GMAF0.3659
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19110211OA-icon.png] rs7961894, rs12485738 and rs2138852 together accounted for 4%-5% of the variance in mean platelet volume, which is increased in myocardial and cerebral infarction and is an independent and strong predictor for postevent morbidity and mortality
OMIM612574
DescMEAN PLATELET VOLUME QUANTITATIVE TRAIT LOCUS 2; MPVQTL2
Variant
Relatedalso
GWAS snp
PMID [PMID 19820697OA-icon.png]
Trait MPV
Title A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Risk Allele A
P-val 6E-31
Odds Ratio 0.02 [0.013-0.017] fl increase




GET Evidence
rs12485738
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.695312
summary